| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| J S Liu, T P Molchanova, L H Gu, J B Wilson, P Hopmeier, W Schnedl, E Balaun, G J Krejs, T H Huisma. Hb Graz or alpha 2 beta 2(2)(NA2)His-->Leu; a new beta chain variant observed in four families from southern Austria. Hemoglobin. vol 16. issue 6. 1993-02-19. PMID:1487420. |
hb graz or alpha 2 beta 2(2)(na2)his-->leu; a new beta chain variant observed in four families from southern austria. |
1993-02-19 |
2023-08-11 |
Not clear |
| J S Liu, T P Molchanova, L H Gu, J B Wilson, P Hopmeier, W Schnedl, E Balaun, G J Krejs, T H Huisma. Hb Graz or alpha 2 beta 2(2)(NA2)His-->Leu; a new beta chain variant observed in four families from southern Austria. Hemoglobin. vol 16. issue 6. 1993-02-19. PMID:1487420. |
the second variant was identical to hb sherwood forest or alpha 2 beta 2(104)(g6)arg-->thr; it is believed that this may be the second observation of this abnormal hemoglobin. |
1993-02-19 |
2023-08-11 |
Not clear |
| S Negri Arjona, J Maldonado Eloy-Garcia, T P Molchanova, J B Wilson, L H Gu, T H Huisma. Hb Brockton [alpha 2 beta 2(138)(H16)Ala-->Pro] observed in a Spanish girl. Hemoglobin. vol 16. issue 6. 1993-02-19. PMID:1487422. |
hb brockton [alpha 2 beta 2(138)(h16)ala-->pro] observed in a spanish girl. |
1993-02-19 |
2023-08-11 |
Not clear |
| F F Costa, M S Figueredo, M F Sonati, E M Kimura, C S Martin. The IVS-I-110 (G-->T) and codon 39 (C-->T) beta-thalassemia mutations in association with alpha-thal-2 (-3.7 Kb) and Hb Hasharon [alpha 47(CE5)Asp-->His] in a Brazilian patient. Hemoglobin. vol 16. issue 6. 1993-02-19. PMID:1487425. |
the ivs-i-110 (g-->t) and codon 39 (c-->t) beta-thalassemia mutations in association with alpha-thal-2 (-3.7 kb) and hb hasharon [alpha 47(ce5)asp-->his] in a brazilian patient. |
1993-02-19 |
2023-08-11 |
Not clear |
| G D Efremo. Hemoglobinopathies in Yugoslavia: an update. Hemoglobin. vol 16. issue 6. 1993-02-19. PMID:1487426. |
five different alpha chain variants among 21 families, 15 different beta chain variants among 53 families, one delta chain variant in one family, one variant with a deleted residue in one family, and two types of hb lepore among 122 families, have been observed. |
1993-02-19 |
2023-08-11 |
Not clear |
| P T Biessels, G A Berbers, G C Broeders, R Landsvater, H G Huisman, W K Bleeker, J C Bakke. Detection of erythrocyte membrane components in hemoglobin-based blood substitutes. Clinica chimica acta; international journal of clinical chemistry. vol 212. issue 3. 1993-02-05. PMID:1477974. |
hb solutions prepared by filtration of red blood cells, gradually swollen in hypotonic buffer, contained 0.25% of the original amount of phospholipid and no detectable glycophorin alpha. |
1993-02-05 |
2023-08-11 |
human |
| P T Biessels, G A Berbers, G C Broeders, R Landsvater, H G Huisman, W K Bleeker, J C Bakke. Detection of erythrocyte membrane components in hemoglobin-based blood substitutes. Clinica chimica acta; international journal of clinical chemistry. vol 212. issue 3. 1993-02-05. PMID:1477974. |
for hb solutions prepared in a similar way from red blood cells lysed in water, the values for phospholipid and glycophorin alpha were 2.5% and 0.06%, respectively. |
1993-02-05 |
2023-08-11 |
human |
| P T Biessels, G A Berbers, G C Broeders, R Landsvater, H G Huisman, W K Bleeker, J C Bakke. Detection of erythrocyte membrane components in hemoglobin-based blood substitutes. Clinica chimica acta; international journal of clinical chemistry. vol 212. issue 3. 1993-02-05. PMID:1477974. |
the determination of both glycophorin alpha and phospholipid gives a useful indication of the purity of hb solutions. |
1993-02-05 |
2023-08-11 |
human |
| M D Gross, S M Gapstur, J D Belcher, G Scanlan, J D Potte. The identification and partial characterization of acetaldehyde adducts of hemoglobin occurring in vivo: a possible marker of alcohol consumption. Alcoholism, clinical and experimental research. vol 16. issue 6. 1993-01-27. PMID:1471764. |
a comparison of the observed mass for the peptides with the theoretical masses for acetaldehyde-modified hb peptides suggested that the peptides were ach-modified alpha and beta chain n-termini of hb. |
1993-01-27 |
2023-08-11 |
Not clear |
| Y J Fei, R Oner, G Bözkurt, L H Gu, C Altay, A Gurgey, S Fattoum, E Baysal, T H Huisma. Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observations. Acta haematologica. vol 88. issue 2-3. 1993-01-21. PMID:1281602. |
hb h disease caused by a homozygosity for the aataaa-->aataag mutation in the polyadenylation site of the alpha 2-globin gene: hematological observations. |
1993-01-21 |
2023-08-11 |
Not clear |
| V Divoky, E Bissé, J B Wilson, L H Gu, H Wieland, I Heinrichs, J F Prior, T H Huisma. Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia. Biochimica et biophysica acta. vol 1180. issue 2. 1993-01-21. PMID:1463768. |
one chromosome of the propositus and one of his father's carried the gtg-->ggg mutation at codon 126 leading to the synthesis of hb dhonburi or alpha 2 beta (2)126(h4)val-->gly; this variant is slightly unstable and is associated with mild thalassemic features. |
1993-01-21 |
2023-08-11 |
Not clear |
| M E Fabry, R L Nagel, A Pachnis, S M Suzuka, F Costantin. High expression of human beta S- and alpha-globins in transgenic mice: hemoglobin composition and hematological consequences. Proceedings of the National Academy of Sciences of the United States of America. vol 89. issue 24. 1993-01-19. PMID:1465454. |
because mouse alpha chains inhibit hemoglobin (hb) s polymerization, we bred the mice to heterozygosity for a mouse alpha-globin deletion. |
1993-01-19 |
2023-08-11 |
mouse |
| M E Fabry, R L Nagel, A Pachnis, S M Suzuka, F Costantin. High expression of human beta S- and alpha-globins in transgenic mice: hemoglobin composition and hematological consequences. Proceedings of the National Academy of Sciences of the United States of America. vol 89. issue 24. 1993-01-19. PMID:1465454. |
transgenic alpha h beta s[beta mdd] mice had normal hematocrit and hb and somewhat elevated reticulocytes (6% vs. 3% for control), whereas the mice carrying the alpha-globin deletion (alpha h beta s[alpha md beta mdd]) had a normal hematocrit and hb and more elevated reticulocytes (10.3 +/- 7.6% vs. 3.4 +/- 1.0%). |
1993-01-19 |
2023-08-11 |
mouse |
| M E Fabry, R L Nagel, A Pachnis, S M Suzuka, F Costantin. High expression of human beta S- and alpha-globins in transgenic mice: hemoglobin composition and hematological consequences. Proceedings of the National Academy of Sciences of the United States of America. vol 89. issue 24. 1993-01-19. PMID:1465454. |
expression of the transgene restored a normal distribution of erythrocyte densities when compared to thalassemic mice; however, the average mean corpuscular hb concentration of alpha h beta s[beta mdd] mice increased to 35.7 g/dl (vs. control 33.7 g/dl) whereas that of alpha h beta s[alpha md beta mdd] mice was further elevated to 36.3 g/dl. |
1993-01-19 |
2023-08-11 |
mouse |
| M E Fabry, R L Nagel, A Pachnis, S M Suzuka, F Costantin. High expression of human beta S- and alpha-globins in transgenic mice: hemoglobin composition and hematological consequences. Proceedings of the National Academy of Sciences of the United States of America. vol 89. issue 24. 1993-01-19. PMID:1465454. |
the higher values of the mean corpuscular hb concentration and intrinsic po2 at midsaturation, which favor in vivo sickling, may explain the slightly more severe hematological picture in alpha h beta s[alpha md beta mdd] mice. |
1993-01-19 |
2023-08-11 |
mouse |
| T P Molchanova, J B Wilson, L H Gu, R D Hain, L S Chang, A O Poon, T H Huisma. A second observation of the fetal methemoglobin variant Hb F-M-Fort Ripley or alpha 2G gamma 2(92)(F8)His----Tyr. Hemoglobin. vol 16. issue 5. 1992-12-14. PMID:1385361. |
a second observation of the fetal methemoglobin variant hb f-m-fort ripley or alpha 2g gamma 2(92)(f8)his----tyr. |
1992-12-14 |
2023-08-11 |
Not clear |
| S Abbes, A M'Rad, P A Fitzgerald, P Dormer, Y Blouquit, J Kister, F Galacteros, H Wajcma. HB Al-Ain Abu Dhabi [alpha 18(A16)Gly----Asp]: a new hemoglobin variant discovered in an Emiratee family. Hemoglobin. vol 16. issue 5. 1992-12-14. PMID:1428941. |
hb al-ain abu dhabi [alpha 18(a16)gly----asp]: a new hemoglobin variant discovered in an emiratee family. |
1992-12-14 |
2023-08-11 |
Not clear |
| S Abbes, A M'Rad, P A Fitzgerald, P Dormer, Y Blouquit, J Kister, F Galacteros, H Wajcma. HB Al-Ain Abu Dhabi [alpha 18(A16)Gly----Asp]: a new hemoglobin variant discovered in an Emiratee family. Hemoglobin. vol 16. issue 5. 1992-12-14. PMID:1428941. |
the structural determination, performed by reversed phase high performance liquid chromatography and amino acid sequencing, revealed a new variant that we named hb al-ain abu dhabi [alpha 18(a16) gly----asp]. |
1992-12-14 |
2023-08-11 |
Not clear |
| T C Liu, J S Yen, J S Shen, Y H Chen, L S Lee, P H Chen, J G Chan. Rapid molecular diagnosis of hemoglobin variants by RT-PCR of reticulocyte mRNA and direct sequencing. Hemoglobin. vol 16. issue 5. 1992-12-14. PMID:1428942. |
the amino acid substitution of hb g-taichung is due to a g----c mutation at codon 74 of the alpha 1-globin gene, that of hb j-meinung to a g----a substitution at codon 56 of the beta-globin gene, and that of hb kaohsiung (or new york) to a t----a substitution at codon 113 of the beta-globin gene. |
1992-12-14 |
2023-08-11 |
Not clear |
| C W Su, S Liang, R Liang, X J Wen, C N Tan. Hb H disease in association with the silent beta chain variant Hb Hamilton or alpha 2 beta 2(11)(A8)Val----Ile. Hemoglobin. vol 16. issue 5. 1992-12-14. PMID:1428944. |
hb h disease in association with the silent beta chain variant hb hamilton or alpha 2 beta 2(11)(a8)val----ile. |
1992-12-14 |
2023-08-11 |
Not clear |